Safety and Tolerability of Oral LCL161 in Japanese Adult Patients With Advanced Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

November 30, 2013

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Neoplasms
Interventions
DRUG

LCL161

Patients will receive oral LCL161 once a week until unacceptable toxicity, disease progression and/or withdrawal of consent.

DRUG

Paclitaxel

Patients will receive weekly paclitaxel as intravenous infusion over 1 hour in combination with LCL161, from cycle 2 in dose escalation part or from the first cycle in dose expansion part, and will continue it until unacceptable toxicity, disease progression and/or withdrawal of consent.

Trial Locations (2)

466-8560

Novartis Investigative Site, Nagoya

650-0017

Novartis Investigative Site, Kobe

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY